MolNFT v1 · #180938 · protein
Model of MHC class ib H2-M3 with mouse ND1 N-terminal heptapeptide, ala mutant, refined at 1.70 ångströms resolution
7LFJ · Histocompatibility 2, M region locus 3: “Model of MHC class ib H2-M3 with mouse ND1 N-terminal heptapeptide, ala mutant, refined at 1.70 ångströms…”. X-ray diffraction, 2 ligands (NAG, NA), 11 pockets (best druggability 0.76).…
- PDB
- 7LFJ
- Type
- protein
- Length
- 764 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Histocompatibility 2, M region locus 3; Beta-2-microglobulin; Heptapeptide from…
- EC
- 7.1.1.2
- UniProt
- Q31093, P01887, P03888
- Ligands
- NAG, NA
- Pockets
- 11 · best druggability 0.76
Structure
x-ray diffraction · 3 distinct chains · 20% helix, 42% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, D | Histocompatibility 2, M region locus 3 | protein | 276 | 27% helix, 40% strand | Q31093 |
| B, E | Beta-2-microglobulin | protein | 99 | 0% helix, 49% strand | P01887 |
| C, F | Heptapeptide from NADH-ubiquinone oxidoreductase chain 1 (EC 7.1.1.2) | protein | 7 | 0% helix, 0% strand | P03888 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
11 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 136 | 0.76 | 0.94 | 24 | empty |
| 2 | 531 | 0.69 | 0.79 | 49 | empty |
| 3 | 660 | 0.68 | 0.77 | 68 | empty |
| 4 | 382 | 0.63 | 0.78 | 47 | empty |
| 5 | 242 | 0.57 | 0.78 | 37 | empty |
Interfaces
7 interfaces between chains.
- D–E · 1317 Ų buried · 24 hydrogen bonds · protein-protein
- A–B · 1297 Ų buried · 25 hydrogen bonds · protein-protein
- A–D · 877 Ų buried · 5 hydrogen bonds · protein-protein
- A–C · 784 Ų buried · 8 hydrogen bonds · protein-protein
- D–F · 732 Ų buried · 7 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 disulfide, 2 modified, 1 glycan (disulfide, formylation, N-glycosylation).
Compared structures
- 7LFJ · MODEL OF MHC CLASS Ib H2-M3 WITH MOUSE ND1 N-TERMINAL HEPTAPEPTIDE, ALA MUTANT, REFINED… · the same entry in another collection · chain F against F, TM-score 1.00
- P01887 · AlphaFold monomer V2.0 prediction for beta-2-microglobulin (P01887) · a predicted model of the same protein · chain E against A, TM-score 0.99
- P03888 · AlphaFold monomer V2.0 prediction for NADH-ubiquinone oxidoreductase chain 1 (P03888) · a predicted model of the same protein · chain C against A, TM-score 0.46
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt Q31093
- Every structure of UniProt P01887
- Every structure of UniProt P03888
- Elsewhere: RCSB PDB 7LFJ · PDBe 7LFJ · UniProt Q31093 · UniProt P01887 · UniProt P03888
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.